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Dive into the research topics of 'Rett syndrome and beyond: Recurrent spontaneous and familial MECP2 mutations at CpG hotspots'. Together they form a unique fingerprint.- Sort by
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Mimi Wan, Stephen Sung Jae Lee, Xianyu Zhang, Isa Houwink-Manville, Hae Ri Song, Ruthie E. Amir, Sarojini Budden, Sakku Bai Naidu, Jose Luiz P. Pereira, Ivan F.M. Lo, Huda Y. Zoghbi, N. Carolyn Schanen, Uta Francke
Research output: Contribution to journal › Article › peer-review